Donepezil And Memantine, Key Dementia Drugs, Should Be Used More: Study

By Kate Kelland

LONDON, March 7 (Reuters) – Pfizer’s dementia drug Aricept, already commonly used to treat mild to moderate Alzheimer’s disease, can also help patients with severe disease and should be used more widely and for longer, according to research published on Wednesday.

British scientists who studied the possible longer-term benefits of giving Aricept suggested that extending treatment could help twice as many Alzheimer’s sufferers worldwide.

The study also looked at another commonly used dementia drug called memantine, which is sold in the United States under the brand Namenda by Forest Laboratories and Germany’s Merz, and in Britain under the brand Ebixa by Danish group Lundbeck .

It found that keeping patients with moderate to severe Alzheimer’s on Aricept, or donepezil as it is known generically, or starting them on memantine treatment, meant they had significantly better cognitive and function abilities than patients taking a placebo or dummy pill.

An estimated 18 million people worldwide suffer from Alzheimer’s disease, which is the most common form of dementia. It is fatal brain disease that affects memory, thinking, behaviour and the ability to handle daily activities and is placing an increasingly heavy burden on societies and economies across the world.

According to the World Health Organisation, some 35 million people worldwide have dementia, and Alzheimer’s Disease International predicts that as populations age, dementia cases will almost double every 20 years to around 66 million in 2030 and 115 million in 2050.

The study, published in the New England Journal of Medicine, involved 295 Alzheimer’s patients in Britain who were assigned to one of four separate groups – one continuing to take donepezil, one stopping donepezil and getting a placebo, one stopping donepezil and starting memantine, and a fourth taking both drugs together.

Robert Howard, a professor at King’s College London who led the trial, said it was the first to show the value of continued drug treatment for patients with moderate to severe Alzheimer’s.

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Commonly used dementia drugs can help more patients with Alzheimer’s

Public release date: 7-Mar-2012 [ | E-mail | Share ]

Contact: Katherine Barnes katherine.barnes@kcl.ac.uk 44-207-848-3076 King’s College London

The dementia drug donepezil (Aricept), already widely used to treat mild to moderate Alzheimer’s disease, can also help in moderate to severe patients, according to a report funded by the UK Medical Research Council (MRC) and the Alzheimer’s Society. The study suggests that extending treatment to this group could help treat twice as many sufferers worldwide. Encouragingly, the drug has greater positive benefits for patients more severely affected than for those in the earlier stages of dementia.

It is estimated that 18 million people worldwide suffer from Alzheimer’s disease, which is the most common cause of dementia. According to the World Health Organization, of the 35 million people currently living with dementia globally, 58% live in low- and middle-income countries and by 2050 this figure is projected to reach 71% of the total.

The multi-centre UK study, led by Professor Robert Howard at King’s College London, is the first trial to demonstrate the value of continued drug intervention for those patients with moderate to severe Alzheimer’s disease who have deteriorated beyond the point where donepezil is currently recommended.

The study, to be published in the New England Journal of Medicine, looked at two drugs: donepezil and memantine. Donepezil is the most commonly prescribed of the dementia drugs and is recommended for patients at the earliest stages of Alzheimer’s disease. Doctors are currently advised to stop prescribing donepezil when the disease progresses to become moderate to severe and until now there has been no clear evidence that continuing treatment is of benefit to patients.

Over the course of the trial, patients who continued to take donepezil showed considerably less decline in cognition memory, orientation, language function and function (retained ability to carry out simple daily tasks and self-care) than those taking a placebo drug. The benefits seen with continued treatment were clinically important and were greater than those previously seen in patients with less severe Alzheimer’s disease. Whilst the effect was slightly smaller, starting memantine treatment also resulted in significantly better cognitive and functional abilities compared with those taking a placebo.

Professor Robert Howard, lead author from the Institute of Psychiatry at King’s says: “As patients progress to more severe forms of Alzheimer’s disease, clinicians are faced with a difficult decision as to whether to continue or not with dementia drugs and, until now, there has been little evidence to guide that decision. For the first time, we have robust and compelling evidence that treatment with these drugs can continue to help patients at the later, more severe stages of the disease. We observed that patients who continued taking donepezil were better able to remember, understand, communicate and perform daily tasks for at least a year longer than those who stopped taking the drugs. These improvements were noticeable to patients, their caregivers and doctors. Both donepezil and memantine will soon be off patent and available in very cheap generic preparations. These findings will greatly increase the numbers of patients in the developed and developing world that we are able to treat.”

Professor Nick Fox, MRC Senior Clinical Fellow at the Institute of Neurology, University College London, says: “The number of people with Alzheimer’s disease and other forms of dementia is reaching critical levels. It has never been more important to invest in research which will enable doctors to make informed decisions based on the best evidence possible when deciding what treatments to give patients. The MRC has an ongoing commitment to the development of effective, safe treatments that will improve the quality of life for people with Alzheimer’s disease and their care givers.”

Professor Clive Ballard, Director of Research at Alzheimer’s Society, says: “Thanks to the Alzheimer’s drug donepezil, tens of thousands of people in the early to moderate stages of the condition are able to recognise their family for longer, play with their grandchildren and make vital plans for the future. This major new trial now shows that there could also be significant benefits on continuing the treatment into the later stages too. There are 750,000 people with dementia in the UK yet currently prescription levels of Alzheimer’s drugs are still low. If this is to change we have to improve the shocking diagnosis rates and ensure everyone is given the opportunity to try treatments.”

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Dementia To Cost $200 Billion in 2012, Report Finds

The bill for taking care of people with Alzheimer’s and other dementias will reach $200 billion this year in the United States, including $140 billion paid by Medicare and Medicaid, the Alzheimers Association said on Thursday.

The group estimated that 800,000 Americans have Alzheimer’s and live alone, and as many as half dont have any set person to help care for them.

“Alzheimer’s is already a crisis and it’s growing worse with every year,” Harry Johns, president and CEO of the Alzheimer’s Association, said in a statement. Health officials and policymakers already dread the coming crisis from the disease, which has no cure and no effective treatment.

In its annual report, the Alzheimers Association said Medicare payments for a dementia patient than for seniors without Alzheimer’s or another dementia. lzheimer’s and other dementias are nearly three times higher and Medicaid payments 19 times higher The price tag is 19 times higher for Medicaid patients with dementia.

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Alzheimer’s, Dementia Care to Cost U.S. $200 Billion This Year

THURSDAY, March 8 (HealthDay News) — Caring for people with Alzheimer’s disease and other types of dementia will cost the United States about $200 billion this year, a total that includes $140 billion paid by Medicare and Medicaid, new statistics released Thursday show.

Medicaid payments are 19 times higher for seniors with Alzheimer’s and other dementias and Medicare payments for the conditions are nearly three times higher, compared to payments for other patients, according to the “2012 Alzheimer’s Disease Facts and Figures” report from the Alzheimer’s Association.

Nearly 30 percent of people with Alzheimer’s and other dementias are covered by both Medicare and Medicaid, compared to 11 percent of people without the conditions. This means that Medicare and Medicaid costs associated with Alzheimer’s and other dementias will continue to rise as baby boomers age, the report said.

“Alzheimer’s is already a crisis, and it’s growing worse with every year,” Harry Johns, president and CEO of the Alzheimer’s Association, said in an association news release.

“While lives affected and care costs soar, the cost of doing nothing is far greater than acting now. Alzheimer’s is a tremendous cost-driver for families and for Medicare and Medicaid. This crisis simply cannot be allowed to reach its maximum scale because it will overwhelm an already overburdened system,” Johns added.

Most people with Alzheimer’s and other dementias have at least one other serious chronic health problem, and Alzheimer’s acts as a “cost multiplier” on these other diseases, according to the report.

For example, the statistics showed a senior with diabetes and Alzheimer’s costs Medicare 81 percent more than a senior with diabetes alone. And a senior with cancer and Alzheimer’s costs Medicare 53 percent more than a senior with cancer alone.

Mental impairment in patients with Alzheimer’s and other dementias complicates the management of care, resulting in more and longer hospital stays, the authors noted in the news release.

“This disease must be addressed on parallel tracks: supporting research to find treatments that cure, delay or prevent the disease, and offering assistance and support to the more than 5 million Americans now living with Alzheimer’s and their more than 15 million caregivers,” Johns said.

“This is what the National Alzheimer’s Plan is all about. Caring for people with Alzheimer’s and other dementias costs America $200 billion in just one year. By committing just 1 percent of that cost, $2 billion, to research, it could begin to put the nation on a path to effective treatments and, ultimately, a cure,” he noted.

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Dementia patient tracker trialled

7 March 2012 Last updated at 19:23 ET

The use of a tracking device to help people with dementia maintain a degree of independence is to be trialled by NHS Dumfries and Galloway.

The Buddi system allows those wearing the GPS-linked equipment to stay active without fear of getting lost.

The tracker can also be activated to call for emergency help, and to alert carers and relatives to a fall.

The health board’s nurse director, Hazel Boreland, said it could help to keep people “in a safe environment”.

She described it as an “innovative system” which could give added peace of mind to carers and families.

“Anything that can help patients with dementia maintain an increased level of safe independence has to be something that we test,” she said.

“So that is why we are giving it a go.”

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Study finds key dementia drugs should be used more

LONDON (Reuters) – Pfizer’s dementia drug Aricept, already commonly used to treat mild to moderate Alzheimer’s disease, can also help patients with severe disease and should be used more widely and for longer, according to research published on Wednesday.

British scientists who studied the possible longer-term benefits of giving Aricept suggested that extending treatment could help twice as many Alzheimer’s sufferers worldwide.

The study also looked at another commonly used dementia drug called memantine, which is sold in the United States under the brand Namenda by Forest Laboratories and Germany’s Merz, and in Britain under the brand Ebixa by Danish group Lundbeck.

It found that keeping patients with moderate to severe Alzheimer’s on Aricept, or donepezil as it is known generically, or starting them on memantine treatment, meant they had significantly better cognitive and function abilities than patients taking a placebo or dummy pill.

An estimated 18 million people worldwide suffer from Alzheimer’s disease, which is the most common form of dementia. It is fatal brain disease that affects memory, thinking, behaviour and the ability to handle daily activities and is placing an increasingly heavy burden on societies and economies across the world.

According to the World Health Organisation, some 35 million people worldwide have dementia, and Alzheimer’s Disease International predicts that as populations age, dementia cases will almost double every 20 years to around 66 million in 2030 and 115 million in 2050.

The study, published in the New England Journal of Medicine, involved 295 Alzheimer’s patients in Britain who were assigned to one of four separate groups – one continuing to take donepezil, one stopping donepezil and getting a placebo, one stopping donepezil and starting memantine, and a fourth taking both drugs together.

Robert Howard, a professor at King’s College London who led the trial, said it was the first to show the value of continued drug treatment for patients with moderate to severe Alzheimer’s.

While donepezil is commonly prescribed for patients in the early stages of the disease, doctors in some countries, including Britain, are advised to stop prescribing the drug to patients once their disease has progressed to become more severe.

“As patients progress to more severe forms of Alzheimer’s disease, clinicians are faced with a difficult decision as to whether to continue or not with dementia drugs and, until now, there has been little evidence to guide that decision,” Howard told reporters at a briefing abut his findings.

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Pregnancy May Protect Against MS, Study Says

WEDNESDAY, March 7 (HealthDay News) — New research suggests that pregnancy may decrease women’s risk of developing multiple sclerosis.

“Even one pregnancy was associated with nearly a halving of risk [of developing MS symptoms],” said study author Anne-Louise Ponsonby, head of the environmental and genetic epidemiology and research group at Murdoch Children’s Research Institute in Melbourne, Australia. The team also found that women who were pregnant two or more times had only one-quarter of the risk of developing MS symptoms as those who were never pregnant.

The study was published online March 7 in the journal Neurology.

Previous research has found that pregnancy in women who already have MS — an autoimmune disorder — is linked with lower rates of relapse.

Ponsonby’s team found an association between pregnancy and a lower risk of MS symptoms, not a direct cause-and-effect link. They say, however, that this association may help explain why the incidence of MS in women has inched up over the past few decades, as more women delay pregnancy or have fewer babies or none at all.

The researchers evaluated information on 282 Australian men and women, aged 18 to 59, who had MS symptoms — which can include fatigue, numbness, balance or walking problems — but had not been diagnosed with the disease. The researchers looked at both the number of live births and pregnancies lasting at least 20 weeks in the women. They also recorded the number of children born to men. They compared those statistics to 542 men and women without MS symptoms.

No link was found between the number of children men had and their risk of MS symptoms. There was an association with women, however: the risk of developing MS symptoms decreased as the number of pregnancies increased.

The researchers couldn’t say exactly why pregnancy may lower MS risk, but they speculated it could be the increase in estrogen during pregnancy or the effect pregnancy has on inflammatory genes involved in MS.

The study was funded by the National Multiple Sclerosis Society and other organizations.

Women are more likely than men to develop MS. Having a close relative with MS also increases your risk. About 400,000 people in the United States have MS, according to the National Multiple Sclerosis Society.

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Pregnancy seems to protect against multiple sclerosis

Women who have been pregnant two or more times had a reduced risk of developing the disease, study finds. (Paul Sakuma / Associated Press)

March 7, 2012, 1:17 p.m.

Pregnancy is known to cause a remission in symptoms of multiple sclerosis in women who have MS prior to becoming pregnant. Now a study has found that multiple pregnancies may help prevent MS from ever developing.

The study, published online Wednesday in the journal Neurology, reviewed information on 282 men and women who received a diagnosis of central nervous demyelination. That’s a condition that reflects early symptoms of MS but falls short of an actual MS diagnosis. The researchers compared those people to 542 healthy men and women.

They found that women who have been pregnant two or more times had a reduced risk of developing the disease. Women who had five or more pregnancies had one-twentieth the risk of developing MS compared with women who were never pregnant. There was no effect on men regarding their number of offspring and onset of the disease.

Rates of MS have increased over the last several decades. This increase could reflect the fact that women are having fewer children, said the lead author of the study, Anne-Louise Ponsonby of Murdoch Children’s Research Institute in Melbourne, Australia. It’s not clear what it is about pregnancy that protects against MS or causes its temporary remission. It’s likely that hormones play a role, and studies are underway looking at estrogen as a treatment for the illness. It’s also possible that immune changes that take place during pregnancy alter symptoms of the disease as well as the risk of developing it.

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From ‘Refrigerator Mothers’ to untangling the genetic roots of autism

Public release date: 7-Mar-2012 [ | E-mail | Share ]

Contact: Michael Bernstein m_bernstein@acs.org 202-872-6042 American Chemical Society

With the “Refrigerator Mother” notion about the cause of autism a distant and discredited memory, scientists are making remarkable progress in untangling the genetic roots of the condition, which affects millions of children and adults, according to an article in the current edition of Chemical & Engineering News. C&EN is the weekly newsmagazine of the American Chemical Society, the world’s largest scientific society.

In the story, C&EN Associate Editor Lauren K. Wolf points out that most people in the 1960s believed autism resulted from a lack of maternal warmth and emotional attachment. It was a hypothesis popularized by Austrian-born American child psychologist and writer Bruno Bettelheim. Now scientists around the globe are focusing on genes that have been implicated in autism and related conditions, collectively termed “autism spectrum disorders.” That research may solve mysteries about autism, which affects 1 in 110 children in the U.S. Among them: what causes autism, why does it affect more boys than girls and what can be done to prevent and treat it?

C&EN explains that scientists now have solidly implicated certain genes as being involved in autism. Most of those genes play a role in the transmission of signals through the junctions or “synapses” between nerve cells. Synapses are the territory where one nerve releases a chemical signal that hands off messages to an adjoining nerve. The human brain has an estimated 1,000 trillion synapses, and they are hot spots for miscommunications that underpin neurological disorders like autism. Scientists now are gleaning information on what those genes do, what brain circuits they affect and how the proteins they produce function. In doing so, they are paving the way for future medications for autism spectrum disorders.

###

The American Chemical Society is a nonprofit organization chartered by the U.S. Congress. With more than 164,000 members, ACS is the world’s largest scientific society and a global leader in providing access to chemistry-related research through its multiple databases, peer-reviewed journals and scientific conferences. Its main offices are in Washington, D.C., and Columbus, Ohio.

To automatically receive news releases from the American Chemical Society contact newsroom@acs.org.

AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.

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Intermittent fasting promotes brain health

By Michelle Bosmier

According to a new study carried out at the National Institute on Aging in Baltimore, fasting for one or two days each week may help improve the condition of individuals suffering from Alzheimer's and Parkinson's. Researchers have found that stopping nearly all food intake for short periods of time triggers a protection mechanism within the brain which also works against the effects of neurodegenerative disorders.

Calorie intake impacts the brain

Professor Mark Mattson, lead author of the study and professor of neuroscience at the Johns Hopkins University School of Medicine, explained at the American Association for the Advancement of Science in Vancouver that "reducing your calorie intake could help your brain, but doing so by cutting your intake of food is not likely to be the best method of triggering this protection. It is likely to be better to go on intermittent bouts of fasting, in which you eat hardly anything at all, and then have periods when you eat as much as you want. In other words, timing appears to be a crucial element to this process." Read more...

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Anti-cancer fungus found to naturally eat away plastic waste

by: Jonathan Benson

What if it was possible to eliminate much of the world's otherwise very-slowly-biodegrading plastic waste using a natural Amazonian fungus? Well, it just might be, thanks to research conducted by Jonathan Russell and colleagues from Yale University's Department of Molecular Biophysics and Biochemistry, who recently discovered that Pestalotiopsis microspora effectively eats away polyurethane (PUR) plastics, and is capable of using plastic as its sole food source in both aerobic and anaerobic environments.

Entitled Biodegradation of Polyester Polyurethane by Endophytic Fungi, the study aimed to find new potential plant sources of bioremediation, also known as the use of microorganisms to biodegrade and eliminate pollutants that otherwise persist in the environment. Several students attending Yale's annual Rainforest Expedition and Laboratory course collected various samples from the Yasuni National Forest in the Amazon basin, and took them home for testing. Read more...

AyurGold for Healthy Blood

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Anti-cancer fungus found to naturally eat away plastic waste

by: Jonathan Benson

What if it was possible to eliminate much of the world's otherwise very-slowly-biodegrading plastic waste using a natural Amazonian fungus? Well, it just might be, thanks to research conducted by Jonathan Russell and colleagues from Yale University's Department of Molecular Biophysics and Biochemistry, who recently discovered that Pestalotiopsis microspora effectively eats away polyurethane (PUR) plastics, and is capable of using plastic as its sole food source in both aerobic and anaerobic environments.

Entitled Biodegradation of Polyester Polyurethane by Endophytic Fungi, the study aimed to find new potential plant sources of bioremediation, also known as the use of microorganisms to biodegrade and eliminate pollutants that otherwise persist in the environment. Several students attending Yale's annual Rainforest Expedition and Laboratory course collected various samples from the Yasuni National Forest in the Amazon basin, and took them home for testing. Read more...

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Histology replacement? Beckman Institute Researchers Develop Low Cost, Stain-free Optical Technology

Courtesy of Dark Daily:

Pathologists would gain new tool to diagnose cancer faster and more accurately, based upon stain-free analysis of tissue

Reading tissue biopsies with a new stain-free method could eventually help pathologists achieve faster and less subjective cancer detection. Should this technology prove viable, it would also displace many of the longstanding tissue preparation methodologies used today in the histopathology laboratory.

Credit a research team from the Beckman Institute at the University of Illinois (UI) Christie Clinic and at the UI campuses in Urbana and Chicago, with developing this new technology.

They call the technique Spatial Light Interference Microscopy (SLIM). According to a story reported by Futurity.org, the technique uses two beams of light.

Read more: New Way to Look at Tissue Biopsies: Beckman Institute Researchers Develop Low Cost, High-Speed and Stain-free Optical Technology That Could Displace Existing Histopathology Methodologies | Dark Daily http://www.darkdaily.com/new-way-to-look-at-tissue-biopsies-beckman-institute-researchers-develop-low-cost-high-speed-and-stain-free-optical-technology-that-could-displace-existing-histopathology-methodologies-030912#ixzz1oe3Q3qhG

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Welcome to Pathology Malpractice Blog

 

Legal malpractice
A former colleague of mine at Mayo Clinic has started an excellent blog entitled Pathology Malpractice Blog that covers issues related to lessons to be learned from pathology suits and business practices affecting laboratories and pathologists nationwide. 

With about a month under his belt, there are almost 40 posts (and many more on the way) dealing with court rulings, judgements, references to scholarly articles, interesting media stories and commentary to help pathologists successfully navigate the medicolegal world of pathology.  In addition, he has a special interest in client billing and pod labs and would like to use his blog to help pathologists become more informed on these issues, so as to be better positioned to protect patients and themselves from these fraudulent billing schemes.

To my knowledge, the Pathology Malpractice Blog is the first and only blog dealing specifically with these issues.

I think that you will find the content informative written in an easy prose that is relevant to the pathology and laboratory community.

Check out Pathology Malpractice Blog.  Link provided on my sidebar to the right.  You can also follow on Twitter @pathmalblog.

Welcome to the blogosphere!

 

 

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DoD could open huge military tissue archive

The real question here is what is the value of these archives?  What condition are the blocks and tissue in with what I suspect has been suboptimal storage conditions for decades for minable RNA.  There may be some potential but add to the poor quality of the preserved tissue is the issue of likely scant clinical documentation, minimal or no long term follow up information and lack of longitudinal data short of a few registries.

By Patricia Kime - Staff writer Army Times

SILVER SPRING, Md. — Like the vast government warehouse in the closing scene of “Raiders of the Lost Ark,” the 32,000-square-foot repository at the Joint Pathology Center holds thousands of treasures — cardboard boxes stacked floor to ceiling on shelves, containing 32 million tissue samples from ill and injured service members dating to 1917.

That trove of medical detritus could soon be accessible to federal and civilian researchers.

Officials at the Joint Pathology Center, the Pentagon’s main laboratory, research facility and learning institute for pathology, said Tuesday they are working with the Institute of Medicine to determine how to open their tissue repository — the largest in the world — to some scientists.

Considered a national treasurer by researchers, the catalogue of samples holds clues that could lead to medical advancements, said JPC Interim Director Col. Thomas Baker.

“Twenty to 25 years ago, there probably wasn’t a lot of use for this tissue,” Baker said. “But now with molecular studies we can do now, the genoming sequencing … it will allow us to test these samples that will ultimately affect treatment and patient care.”

The paraffin-encased samples include bits and bobs from service members who breathed mustard gas in World War I, contracted the Spanish Flu in 1918, were exposed to Agent Orange in Vietnam and encountered depleted uranium in the sands of Iraq.

There are samples from troops who contracted extremely rare diseases as well as thousands of common diseases — specimens Baker feels should be made available to researchers of other federal agencies if not academia.

“There’s a lot of potential,” he said.

A panel from the Institute of Medicine, the arm of the National Academies that makes recommendations to the federal government on science and health matters, is reviewing the pathology center’s policies and procedures to determine who should have access to the material, how the samples should be used and tested and the ethical considerations of granting access to patients’ biopsies and surgical jetsam.

The report should be out in June, Baker said.

The Joint Pathology Center was created by the 2008 Defense Authorization Act to replace the Armed Forces Institute of Pathology, shuttered as a result of the 2005 round of base closures and realignments.

AFIP was housed on the grounds of Walter Reed Army Medical Center in Washington, D.C.; the JPC is located in Silver Spring. Md., near the soon-to-be-opened National Museum of Health and Medicine and the Walter Reed Army Institute of Research.

JPC has an annual operating budget of about $21.7 million, beyond funding from hospitals and the Defense Department’s Centers of Excellence. Its 36 pathologists and 46 support staff provide pathology consultations for military and Veterans Affairs Department health facilities and military veterinary clinics, as well as electron microscope services and pathology education and research.

 

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Brain of a Pathologist

Courtesy of The 1x Objective.  Word cloud of pathologist brain/pathology reports.

For the past several months have reviewed 100s if not thousands of pathology reports for various purposes, research, education, clinical, LIS configuration, etc... Have to agree with Karl on this.  Outside of "carcinoma" (this likely includes terms such as "negative for carcinoma", cell(s), tumor, words such as "may", "typically" and "case often" are commonly used terms on the very product we produce - a report. 

These vagaries are often very commonly seen and used without reproach and may be seen in many cases in textbooks of cytology, such as statements that begin with "The cells may show features of overall cellular enlargement or be of relatively normal size or mildly enlarged; nuclei may show hyperchromasia or appear normal; nucleoli may or may not be seen".  

Good thing pathology and its accompanying reports are so clear, transparent, direct, easy to quantify and without qualifiers or adverbs...

 

Brain-of-a-pathologist copy

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Pathologists: Embrace the Tumor Board

Dr. Tom Wheeler over at his Medscape blog entitled Lab Line by the Doctor's Doctor has a great note on tumor boards.  The paragraph below pretty much says it all. It is tumor board, not tumor bored and pathologists need to be more of an integral part of these meetings than what I have seen as typical pathologists' roles and reactions to these conferences.

"A number of pathologists that I know view these conferences as a burden and an interruption of their regular work by an activity that is not reimbursed, not to mention the frustration of having cases added at the last minute making it difficult to put together an orderly presentation within time for the meeting.  My view is somewhat different - this is not an interruption of your work it is your work."

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The Future of Clinical Laboratory Courier Services: Technical and Economic Solutions for the Medical Courier Business

FREE Special Edition White Paper

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Download Your FREE Special Report Today!
Simply Complete the Form Below

 

cover-dark-daily-white-paper-courier-servicesIf you consider a million physicians sending patient samples to a quarter million laboratories, and larger hospitals and health systems having multiple laboratories, clinics, and hospitals, as well as from patient service centers (PSCs) to laboratories, it’s easy to understand just how vital the medical courier system is to the healthcare system in general and the clinical laboratory industry specifically.

If you envision the travel of patient specimens as a very complicated web of time and condition-dependent medical samples in constant motion, then the challenges, both technical and economic, become obvious.  Here are some common questions…

How do you track samples?  How are samples handled?  How do you keep costs down?  How do you operate an efficient courier system if, on any given day, you don’t know the number and types of samples that will be transported?

The Dark Report is happy to offer our readers a chance to download our recently published FREE White Paper “The Future of Clinical Laboratory Courier Services: Technical and Economic Solutions for the Medical Courier Business” at absolutely no charge. This report will address these issues above, provide solutions, and include case studies that show how it is currently being handled.

 

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Among other topics, this FREE White Paper specifically addresses:

  1. The economics and fees of a medical lab courier service
  2. Case study, Yale Pathology Labs
  3. Courier transparency and visibility… and much more

For more about closing the medical data gap in your lab, please CLICK HERE.

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Table of Contents

Introduction — Page 3

  • How do you track samples?
  • How are samples handled?
  • How do you keep costs down?
  • How do you operate an efficient courier system?

Chapter 1: Medical Laboratory Courier Logistics — Page 4

  • Physician Ordering
  • Sample Collection & Labeling
  • Sample Delivery
  • Sample Processing
  • Reporting

Chapter 2: Laboratory Specimen Handling and Tracking — Page 7

  • Medical Security
    • HIPAA
    • CAP
    • OSHA
    • TSA
  • Chain of Custody
  • In Transit Tracking

Chapter 3: The Economics of Medical Laboratory Courier Services — Page 11

  • Flat Fee
  • Charge Per Mile
  • Charge per Pickup

Chapter 4: Courier Visibility/Transparency — Page 13

  • Training
  • Uniforms
  • Route Analysis
  • Volume Analysis
  • Logistic Experts

Chapter 5: Case Studies — Page 18

  • Yale Pathology Labs (Yale University)
  • LMC Pathology Services (Las Vegas, NV)

Conclusion — Page 24

Appendices

A-1 About Walter J. Humphrey and Susan M. Uihleiny — Page 26

A-2 About Medifleet — Page 27

A-3 About DARK Daily — Page 28

A-4 About The Dark Intelligence Group, Inc., and THE DARK REPORT — Page 29

A-5 About the Executive War College on Laboratory and Pathology Management — Page 30

A-6 About Mark Terry — Page 32

 Terms of Use — Page 36

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AccelPath Collaborating With Scanner Manufacturers

GAITHERSBURG, MD and WESTWOOD, MA, Mar 06, 2012 (MARKETWIRE via COMTEX) -- AccelPath, LLC ("AccelPath" or the "Company"), a wholly-owned and operating subsidiary of Technest Holdings, Inc., conducts ongoing discussions with several scanner manufacturers.

AccelPath is in discussions with several slide scanner manufacturers to provide their equipment to clinics and hospitals. Scanner deployments will allow the Company to further digitize all aspects of pathology services, allowing advancement of its strategy of providing efficient, timely, fully automated, digital pathology services using existing electronic information technologies. AccelPath will also utilize these relationships to further advance clinics and hospitals with worksite planning, technical services (including software interfaces and scanner operations), network engineering, professional pathology services and post implementation support.

"We are excited about the significant progress being made toward implementation of digital pathology. This would complete a fully digital loop between treating physician and trained pathologist," said Shekhar Wadekar, the Company's Chief Executive Officer. "We are gaining customer acceptance of our workflow solution and this will increase customer awareness and confidence in the Company's product offerings."

About AccelPath AccelPath provides technology solutions that play a key role in delivering information required for diagnosis of diseases and other pathologic conditions with and through its associated institutional pathologists. The medical institutions, with whom the Company partners, prepare comprehensive diagnostic reports of a patient's condition and consult with referring physicians to help determine the most appropriate treatment. Such diagnostic reports enable the early detection of disease, allowing referring physicians to make informed and timely treatment decisions that improve their patients' health in a cost-effective manner. The Company seeks out referring physicians and histology laboratories in need of high-quality pathology interpretations and manages HIPAA-compliant digital case delivery and reporting while developing comprehensive solutions for managing medical information.

AccelPath is currently focused on the $14 billion anatomic pathology market in the US. The Company's business model builds upon the expertise of experienced pathologists to provide seamless, reliable and comprehensive pathology and special test offerings to referring physicians using conventional and digital technologies. The Company establishes longstanding relationships with the referring physicians as a result of focused delivery of its partner's diagnostic services, personalized responses and frequent consultations, and its proprietary flexible information technology, or IT, solutions that are customizable to the referring physicians or laboratories as well as the pathologists' needs. Such diagnostic reports often enable the early detection of disease, allowing referring physicians to make informed and timely treatment decisions that improve their patients' health in a cost-effective manner. AccelPath's IT and communications platform enables it to efficiently and securely deliver diagnostic reports to referring physicians. In addition, AccelPath's IT platform enables close tracking and monitoring of medical statistics.

Technest focuses on the design, research, development and integration of three-dimensional imaging devices and systems primarily in the healthcare industries. The Company also develops solutions and intelligent surveillance devices and systems, as well as three-dimensional facial recognition systems for security and law enforcement agencies. Historically, the Company's largest customers have been the National Institutes of Health and the Department of Defense. The Company's solutions leverage several core proprietary technology platforms, including 3D imaging technologies.

Additional Company information may be found on the Internet at:

http://www.accelpath.com

Forward-Looking Statements This press release contains certain "forward-looking statements" relating to the business of the Company, which can be identified by the use of forward-looking terminology such as "may," "will," "expect," "anticipate," "intend," "estimate," "believe," "project," "continue," "plan," "forecast," or other similar words, or the negative thereof, unless the context requires otherwise. These statements include, but are not limited to, statements about the Company's current discussions with scanner manufacturers, the Company's expected future performance and the acceptance of the Company's product offerings. The results anticipated by any or all of these forward-looking statements may not occur. In addition, these statements reflect management's current views with respect to future events and are subject to numerous risks, uncertainties and other factors that could cause actual results to differ materially from those set forth in or implied by these forward-looking statements. Factors that could affect those results include, but are not limited to, our ability to conclude our discussions with these manufacturers on favorable terms, the acceptance of our solutions in the marketplace, the efforts of our sales force, general economic conditions, and those described in the Company's reports on Forms 8-K, 10-Q and 10-K and proxy statements and information statements, which have been or will be filed by the Company with the Securities and Exchange Commission (the "SEC"), including without limitation under the caption "Risk Factors" in the Company's Annual Report on Form 10-K filed on October 13, 2011. Many of the factors that will determine the outcome of the subject matter of this press release are beyond the Company's ability to control or predict. The Company undertakes no obligation and expressly disclaim any obligation, to revise or publicly update any forward-looking statements, or to make any other forward-looking statements, whether as a result of new information, future events or otherwise.

Source: Marketwatch

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Downside of Digital Medicine

There’s a lot of excitement over the rise of electronic health records — and with good reason. Digital record keeping could make it easier for doctors, hospitals and other providers to share patient information and coordinate care. And that, health policy wonks hope, will reduce costs. Providers will be less likely to order a duplicate test, for instance, if they know a doctor has already performed it. One recent study estimated that wide-scale adoption of electronic medical records could save $8.3 billion annually just by reducing use of medical imaging.

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